Linked Data
ClinVar Variation Id:
2059860
ClinVar RCV Id:
RCV002933928
dbSNP Id:
rs760794410
ExAC:
16:16248782 A / G
gnomAD v2:
16-16248782-A-G
gnomAD v3:
16-16154925-A-G
gnomAD v4:
16-16154925-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16154925A>G , CM000678.2:g.16154925A>G | GRCh38 |
| NC_000016.9:g.16248782A>G , CM000678.1:g.16248782A>G | GRCh37 |
| NC_000016.8:g.16156283A>G | NCBI36 |
| NG_007558.2:g.73547T>C | |
| NG_007558.3:g.73693T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000576204.6:n.852T>C | ||
| ENST00000622290.5:c.*161T>C | ENSP00000483331.2:n.*161T>C | |
| ENST00000205557.12:c.3989T>C MANE Select | ENSP00000205557.7:p.Ile1330Thr | |
| ENST00000640696.1:c.803T>C | ENSP00000492197.1:p.Ile268Thr | |
| ENST00000205557.11:c.3989T>C | ENSP00000205557.7:p.Ile1330Thr | |
| ENST00000456970.6:c.3614T>C | ENSP00000405002.2:n.3614T>C | |
| ENST00000576204.5:n.852T>C | ||
| ENST00000622290.4:c.*1198T>C | ENSP00000483331.1:n.*1198T>C | |
| NM_001171.5:c.3989T>C | NP_001162.4:p.Ile1330Thr | |
| XM_011522479.1:c.3956T>C | XP_011520781.1:p.Ile1319Thr | |
| XM_011522480.1:c.3647T>C | XP_011520782.1:p.Ile1216Thr | |
| XM_011522481.1:c.3647T>C | XP_011520783.1:p.Ile1216Thr | |
| XR_933134.1:n.539-4856A>G | ||
| NM_001351800.1:c.3647T>C | NP_001338729.1:p.Ile1216Thr | |
| NR_147784.1:n.3651T>C | ||
| XM_011522479.2:c.3956T>C | XP_011520781.1:p.Ile1319Thr | |
| XM_011522481.3:c.3647T>C | XP_011520783.1:p.Ile1216Thr | |
| XM_017023212.1:c.3821T>C | XP_016878701.1:p.Ile1274Thr | |
| XM_024450261.1:c.4025T>C | XP_024306029.1:p.Ile1342Thr | |
| NM_001171.6:c.3989T>C MANE Select | NP_001162.5:p.Ile1330Thr |